Results 201 to 210 of about 585,856 (303)

Feasibility of the ICF CoreSets for Autism Strengths and Needs Assessment in NHS diagnostic services in England: protocol for a randomised pilot trial. [PDF]

BMJ Open
Day M, Scargill K, Poole D, Kellar I, Young TA, Bölte S, Clarke S, Lodge KM, Woods A, Freeth M.   +9 more
europepmc   +1 more source

Exploring the Impact of a Culturally Adapted Parent-Directed Training Program for Latine Parents of Children With Autism. [PDF]

Fam Process
Ramos N, Leija V, Cavazos Vela J, Maldonado DB, Perez S.   +4 more
europepmc   +1 more source

Reduced task adaptation and contextual awareness in autistic adults during facial emotion recognition: evidence from mixed-effects modeling and automated facial analysis. [PDF]

Mol Autism
Kirsch S, Drimalla H, Saakyan W, Sajonz BEA, Gritzmann J, Maier S, Fangmeier T, Lin M, Guendelman S, Kaufmann C, Dziobek I, van Elst LT.   +11 more
europepmc   +1 more source

ToM² : Parental Perception of Theory of Mind Abilities in Autistic Children. [PDF]

Autism Res
Joseph LS, Perez M, Perry A, Koller J.
europepmc   +1 more source

Altered neurostructural development in magnetic resonance imaging‐negative pediatric epilepsy: A large‐scale multicenter study of 1919 children

Epilepsia, EarlyView.
Abstract Objective Addressing the poorly understood impact of pediatric epilepsy on neurodevelopment, this large‐scale study delineates age‐ and sex‐stratified neurostructural trajectories in magnetic resonance imaging (MRI)‐negative pediatric epilepsy to identify periods of maximal developmental divergence from healthy controls.
Yingfan Wang, Minghao Li, Huijun Li, Wei Yu, Peilin Jiang, Xinyi Zhou, Ke Hu, Feng Yang, Jiu Chen, Ming Yang, Xiaoshan Wang   +10 more
wiley   +1 more source

Bilingualism, Autism, and Mental Health: Implications for Social Work. [PDF]

Cureus
Abbasian H.
europepmc   +1 more source

Behavioral and epileptic phenotypes in a CHD2‐related developmental delay model

Epilepsia, EarlyView.
Abstract Objective Heterozygous loss‐of‐function mutations in the CHD2 gene, encoding chromodomain helicase DNA‐binding protein 2, are associated with severe childhood onset epilepsy, global developmental delay, and autistic features. Animal models that accurately recapitulate human phenotypes are crucial for understanding rare neurodevelopmental ...
Anat Mavashov, Shaked Turk, Yael Sarusi, Marina Brusel, Rotem Ben Tov Perry, Shir Quinn, Yael Almog, Karni Vilian, Mor Yam, Igor Ulitsky, Moran Rubinstein   +10 more
wiley   +1 more source

Autism Spectrum Disorders and Purinergic Signaling: A Systematic Review of Emerging Insights from Preclinical Studies. [PDF]

J Mol Neurosci
Guha S, Elisha DH, Eshraghi RS, Mittal R, Deth RC, Eshraghi AA.   +5 more
europepmc   +1 more source